Challenges and Breakthroughs in Selective Amide Activation

Abstract In contrast to ketones and carboxylic esters, amides are classically seen as comparatively unreactive members of the carbonyl family, owing to their unique structural and electronic features. However, recent decades have seen the emergence of research programmes focused on the selective activation of amides under mild conditions. In the past four years, this area has continued to rapidly develop, with new advances coming in at a fast pace. Several novel activation strategies have been demonstrated as effective tools for selective amide activation, enabling transformations that are at once synthetically useful and mechanistically intriguing. This Minireview comprises recent advances in the field, highlighting new trends and breakthroughs in what could be called a new age of amide activation.


Introduction
Carbonyl groups are among the most common functionalities in organic molecules and methodologies; allowing their selective functionalisation while concomitantly enabling an increase in molecular complexity are in consistently high demand. In contrast to acyl halides, anhydrides, ketones and esters, amides have historically been considered to be comparatively unreactive. The unique delocalisation of the lone pair of electrons at nitrogen on the π* system, [1][2][3] also known as amidic resonance, is responsible for an increased stabilisation of the electrophilic carbonyl carbon (Scheme 1). [4] This difference in reactivity has led to the perception that amides are significantly less useful functional handles than their ester and acyl halide counterparts. Nonetheless, amides are among the most frequently encountered moieties in functional molecules such as pharmaceutical compounds, bioactive natural products and polymeric materials. Methodologies towards amide activation have proven to facilitate the synthesis of corresponding amidecontaining functional molecules and their analogues. Moreover, highly selective amide activation can also be a valuable tool for late-stage drug modification, thereby benefiting drug discovery and other fields of medicinal chemistry.
Accordingly, synthetic chemists have devoted tremendous efforts to the selective activation of amides since the 19 th century. A comprehensive review on amide activation prior to 2018 was presented by the Maulide group. [5] Work in this fast-developing research field aims to deploy the carboxamide moiety in reactions of diverse nature, where functionalisation occurs either at the carbonyl carbon or at neighbouring positions. [6] Particularly worthy of mention is the trend for such processes to be chemoselective for the carboxamide functionality, even when other, traditionally more reactive carbonyl moieties (such as esters or ketones) are present.
In very recent years, research in this field has stepped into a new age with ever more varied activation strategies and reaction partners. This Minireview highlights breakthroughs in amide activation since 2018, with a focus on significant advances in electrophilic [5] and transition-metalcatalysed amide activation. [7,8] Other strategies initiated by nucleophilic addition [9] or SmI 2 /Sm-redox processes shall be discussed as well.

Electrophilic Amide Activation
The functionalisation of carbonyl derivatives by nucleophilic addition is considered as textbook toolbox chemistry. However, the use of unmodified amides in the same transformations is often challenging, owing to their intrinsic low electrophilicity. Hence, a pre-activation is usually required. Electrophilic amide activation can be achieved with oxophilic reagents, such as phosgene, PCl 5 , oxalyl chloride and triflic anhydride (Tf 2 O). The deployment of Tf 2 O has been established as a powerful strategy, [5] due to its comparably low toxicity, mild reaction protocol and high chemoselectivity. Notably, the mode of reactivity is highly dependent on the nature of the amide, with secondary and tertiary amides showing differences (Scheme 2). [10,11] Initially, the treatment of amides 1 with Tf 2 O leads to iminium triflates 2. Upon further deprotonation, usually mediated by a pyridine base, these are converted to highly electrophilic nitrilium ions 3 for secondary amides, or reactive keteniminium ions 4 in case of their tertiary counterparts. These in situ generated reactive species then set the stage for further transformations. dary amides (5!8) with the inherent nucleophilicity of terminal alkenes 6, Maulide et al. were able to develop a highly chemoselective alkene hydroacylation reaction to access ketones 7 under transition-metal-free conditions (Scheme 3A). [12] Herein, initial electrophilic activation of the amide with triflic anhydride leads to the formation of nitrilium ion 8. This species is prone to attack by an alkene (6) to furnish intermediate 9, ideally suited for intramolecular 1,5-hydride shift. The resulting azonia allene 10 is cleaved by aqueous work up to yield the desired ketone 7. Notably, the reaction tolerated a wide range of functional groups, including several carbonyl derivatives classically considered to be more reactive (cf. "Selected examples" in Scheme 3A).
In a related approach, Huang et al. reported a [4+2]annulation with N-aryl amides 11 and alkenes 12 to afford 3,4-dihydroquinolines 13 (Scheme 3B). [13] The authors also reported that a reductive work up is able to directly yield valuable tetrahydroquinolines 14 in high yields.
Huang et al. further investigated the activation of secondary N-aryl amides 15 by nucleophilic attack of isocyanide 16 (Scheme 4), [14] ultimately leading to 2-substituted 3-iminoindoles 19. Additionally, the authors exploited the electrophilic nature of the newly formed heterocycle for an organocatalysed, asymmetric Mannich-type addition of ketones 17. Despite the presence of two imine groups, a highly enantioselective functionalisation at the C2 position yielding 3-iminoindolines 18 could be achieved in a one-pot fashion.
Electrophilic activation at the ipso-position of amides was further explored for the synthesis of novel classes of heterocycles, once more showcasing the chemical versatility of the evoked intermediates. In 2020, Maulide et al. reported the use of triflic anhydride for the synthesis of unusual 7membered fused heterocycles 21 from α-phthalimido-amides 20 (Scheme 5). [15] From a mechanistic point of view, electrophilic activation takes place at the amide, which is more nucleophilic than the tethered imide. This activation is thought to trigger intramolecular attack by the imide, resulting in formation of an oxazolinium ion 22. solvent of this reaction, was then proposed to yield ketenimine 23, before a two-step ring expansion closed the 7-membered ring, yielding 21 after isomerisation and hydrolysis.
The effect of the substitution pattern of the pyridine bases used in classical triflic-anhydride-mediated amide activation is often not fully understood. [16] For this reason, a range of substituted pyridines is commonly surveyed when optimising reactions involving electrophilic amide activation. [12,15] However, in certain circumstances, the presence of base can even prohibit the desired reactivity. This was observed by Maulide et al. during their endeavour to synthesise alkoxyoxazolium salts 26 (Scheme 6), resulting from intramolecular capture of the electrophilic intermediate by a proximal ester moiety. [17] In this work, control experiments showed that amides 25 with easily accessible αprotons are prone to be deprotonated and attacked by the pyridine base. The formed intermediate 28 inhibits the attack of the ester, leading to starting material recovery after aqueous work up. In contrast, under exclusion of the base, iminium triflate 27 is the predominant active species, and facilitates the desired cyclisation event.
Due to its high selectivity and chemical versatility, the intramolecular capture of intermediates resulting from electrophilic amide activation has also featured in the total syntheses of several natural products. In 2020, Huang et al. exploited the intramolecular attack of a silyl enol ether (29)   on an activated amide for the synthesis of the core structure (30) of stemofoline (31) and stemoburkiline (32) (Scheme 7A). [18] A further example was reported by Christmann and coworkers, who successfully applied the amide activation approach to their concise total synthesis of ilicifoline B 35 (Scheme 7B). [19] Herein, upon activation of amide 33 with POCl 3 and subsequent addition of potassium carbonate and a phase transfer catalyst, tetracyclic scaffold 34 was obtained in excellent yield (affording the natural product after final oxidative dimerisation). Notably, this intriguing reaction proceeds via amide activation and an endo-dig cyclisation, followed by an ester activation mediated exo-trig cyclisation step.

α-Functionalisation of Amides
The α-position of carbonyls possesses intrinsic nucleophilic character that can be exploited for functionalisation through deprotonation by a strong base (e.g. ketone pK a � 24). Amides are no exception, but exhibit low α-acidity (pK a � 35) due to the comparatively weak electron-withdrawing effect of the amide carbonyl. In contrast to the wellestablished methods for polarity reversal of other carbonyl derivatives, the concept of amide umpolung has only recently been extensively explored. [20] Following a previously reported method for amide umpolung using pyridine Noxide derivatives, developed by Maulide et al., [21,22] further investigation of the potential of this reaction has been undertaken.
In the event, a range of heteroatom-based nucleophiles can be coupled to the α-position of amides (36) (Scheme 8A). [23] This work moreover presented new insights into the reaction mechanism: while initial evidence had suggested the direct nucleophilic attack on the enolonium species 39, resulting from addition of a pyridine N-oxide derivative to the in situ generated keteniminium ion 38, indepth experimental and computational studies rather supported the generation of an epoxide intermediate 40 which undergoes interception by the triflate counterion to yield the α-trifloxy amide 41. Indeed, the latter was proven to be an intermediate of this process by independent synthesis and subjection to the reaction conditions. Suitable nucleophiles for displacement of the triflate include halides, alcohols, thiols and tosyl amides. As is common to electrophilic amide activation, functional group tolerance is high with esters, ketones, nitriles and alkenes all being allowed in substrate structure. Remarkably, this method was also successfully employed in the synthesis of α-fluoro amides employing common fluoride salts as nucleophiles (Scheme 8B). Given the high basicity of fluoride, this result is noteworthy. It  opened a door for drug optimisation in medicinal chemistry, as shown by the authors with the ready preparation of hitherto unknown fluoro-citalopram and investigation of its biological properties. [24] The deeper understanding of the reaction mechanism and its intermediates enabled Maulide et al. to further develop an enantioselective CÀ C bond formation process by umpolung (Scheme 9). [25] Herein, the direct formation of αbromo amides (44), via the corresponding α-oxytriflated intermediates (not shown) enabled an asymmetric Nicatalysed Suzuki cross-coupling with arylboronates, yielding chiral α-arylated amides 43.
Maulide also reported the use of alkyl azides (46) in the synthesis of heterocycles (Scheme 10). [26] Upon electrophilic activation of α-arylated acetamides 45 with triflic anhydride, interception of the keteniminium ion by an azide 46 forms the intermediate 47. Enabled by the extrusion of nitrogen gas, intramolecular attack at the electrophilic α-carbon leads to formation of cyclised amidinium triflates 48 or oxazines 49.
Nucleophilic attack at the activated carbonyl position of amides can also facilitate α-functionalisation without relying on umpolung. For example, Evano et al. have shown that the activated intermediates 51, derived from 50, can be brought to reaction with electrophilic fluorine sources to deliver α-fluorocarbonyl derivatives 52 (Scheme 11). [27] Heterocycles (furan and indoles) were well-tolerated.
Sigmatropic rearrangements can also be employed to enable α-functionalisation of amides (53). Recently, Liang et al. reported the synthesis of α-allenyl (57) and α-allyl amides (58) using silylated propargylic (54) and allylic alcohols (55), respectively (Scheme 12A). [28] Therein, following formation of the reactive keteniminium intermediate, oxygen attack followed by desilylation forms a system 56 prone to [3,3]-sigmatropic rearrangement (Claisen-type). Treating activated amides with deuterated dimethyl sulfoxide ([d 6 ]-DMSO), Maulide et al. were able to selectively mono-deuterate the α-position (Scheme 12B). [29] The process was proposed to proceed via a retro-ene reaction of intermediate 60 and delivered the desired product 61 with high degrees of deuteration. Simultaneously, Movassaghi et al. reported the use of sulfoxides 63 for the synthesis of αsulfenylated amides 65 (Scheme 12C). [30] While this process was initially found to only be applicable to α-aryl acetamides, with aliphatic amides providing the retro-ene products shown in Scheme 12B, alteration of the predominant mechanistic pathway by use of an additional electrophilic activator rendered the process general.

Remote Functionalisation of Amides
While electrophilic amide activation was initially employed for functionalisation of the amide carbonyl, and later developments have largely targeted α-functionalisation, most recently, the focus has shifted to the transformation of Previous work by Ghosez had already hinted at the possibility of using N-oxides for the α,β-dehydrogenation of α-branched amides. [19] Based on this report, Maulide et al. were able to develop a general and direct oxidation protocol for the transformation of α-branched-α-aryl amides 66 into the corresponding α,β-unsaturated products 67 (Scheme 13). [31] Remarkably, only the Z-olefins were obtained from this transformation, and the synthetic utility of this class of compounds was demonstrated in a series of onepot derivatisations, including epoxidation (68), β-oxidation (69), conjugate addition (70), and cyclisation to yield butenolides (71).
In order to find a reliable protocol for dehydrogenation of unbranched amides, Maulide turned to alternative reaction conditions and, notably, a different oxidant (Scheme 14). [32] After formation of keteniminium ion 74, nucleophilic addition of benzeneseleninic acid, in presence of an oxidant required to funnel a range of reaction pathways into the same product, leads to intermediate 75.
This species is capable of undergoing a [1,3]-rearrangement to form α-selenated amide 76. Upon in situ elimination, it forms the α,β-unsaturated amides 73. Once more, this transformation can be achieved under mild conditions and with high functional group tolerance, preserving other carbonyl functionalities, such as esters and ketones, and was successfully applied to amide-capped derivatives of drug candidates.
The work shown above reveals how electrophilic amide activation can lead to functionalisation of the "carbonyl side" (ipso-, α-, β-, γ-positions) of the amide precursors. In contrast, manipulations on the "nitrogen side" are rarely explored. An exception was recently published by Maulide et al. employing the unusual combination of Tf 2 O with a strong base (LiHMDS, lithium bis(trimethylsilyl)amide) to form enamides 86 (Scheme 16A) by a direct Ndehydrogenation. [35] From a sequence of labelling studies the authors concluded that, after treatment with Tf 2 O, the triflated species 87 is able to interact with LiHMDS in a (formally oxidative) deprotonation event, leading to intermediates 88 or 89. A second, facile deprotonation by an additional equivalent of LiHMDS then generates the final enamide 86. This reaction features a broad scope, including straightforward functionalisation of drug molecules.

Organocatalytic Electrophilic Amide Activation
Compared to its transition-metal-based counterparts, organocatalytic amide activation has been barely explored. Radosevich and Lipshultz recently published an organophosphorus (P III /P V ) redox-catalysed synthesis of tertiary amides 98 via three-component condensation of carboxylic acids 95, amines 96 and pyridine-N-oxides 97 (Scheme 17). [37] The proposed catalytic cycle is initiated by the reduction of the P V -catalyst 99 with organosilane reagents forming P IIIphosphane 100. Bromination with diethyl (methyl)bromomalonate (DEMBM) forms the reactive intermediate 101, which acts as an activation reagent for both carboxylic acid 95 and amide 103. Upon reaction with carboxylic acid 95, the resulting intermediate 102 is intercepted by amine 96 to furnish amide 103 in situ under regeneration of phosphine oxide 99. In contrast, the activated amide intermediate 104 fragments to form phosphine oxide 99 and the nitrilium ion 105, which can be captured by a pyridine-N-oxide 97 to generate 106. Further rearrangement and rearomatisation (as already demonstrated in previous work by Abramovitch [38] and Movassaghi [16] ) leads to tertiary amide 98. This, to the best of our knowledge, hitherto first organocatalytic strategy might act as the cornerstone for a new generation of electrophilic amide activation approaches.

Iridium-Catalysed Amide Activation
Among the most established strategies for transition-metalcatalysed amide activation, IrCl(CO)(PPh 3 ) 2 -(Vaska's complex, 108) [39] -catalysed hydrosilylation occupies a key place due to its high chemoselectivity for amides in the presence of other functional groups. The Dixon group has been particularly active in exploring the versatility of this catalyst. [7] A prime example of such reactivity can be found in the facile dual iridium-catalysed reductive functionalisation of tertiary amides 107 via hydrosilylation and singleelectron transfer (Scheme 18). [40] In this transformation, reduction of the amide with Vaska's complex 108 in conjunction with TMDS (1,1,3,3-tetramethyldisiloxane) smoothly generates iminium ion 112 in equilibrium at room temperature. The concomitant action of photocatalyst and a stoichiometric reductant under visible light irradiation achieves single-electron reduction to an α-amino radical intermediate 113. Following Giese addition of that radical to electron-deficient alkene 109 and subsequent SET reduction/protonation, the α-aminoalkylated tertiary amine 110 is formed. A variety of tertiary amine architectures can be prepared in moderate to good yields with typically modest diastereoselectivity.
Following this report, a three-component coupling reaction towards the synthesis of α-amino 1,3,4-oxadiazoles 118 with tertiary amides 115, carboxylic acids 116 and (Nisocyanimino) triphenyl-phosphorane (NIITP, 117) was reported by the same group (Scheme 19). [41] Initiated by the selective reduction of amides 115 to the iminium ion 120 using Vaska's complex/TMDS, nucleophilic attack of NIITP (117) leads to formation of the corresponding nitrilium ion 121. After conjunction with a carboxylic acid 116 (or an alternative appropriate C-, S-, or N-centred Brønsted acid), direct aza-Wittig reaction efficiently yields the desired products 118. This method was successfully applied in the late-stage modifications of ten drug molecules, thus demonstrating its efficiency. The key intermediate 120 can also be attacked by difluoro-Reformatsky reagents (BrZnCF 2 R) to afford the medicinally relevant α-difluoroalkylated tertiary amines, as reported recently by the same group. [42] The Dixon group further demonstrated that the reduction of β,γ-unsaturated δ-lactams 123 with Vaska's complex/ TMDS leads to the formation of cyclic dienamines 124 (Scheme 20). [43] These highly reactive species are primed for downstream [4+2]-cycloaddition reactions with a variety of dienophiles 125 to access bridged bicyclic isoquinuclidines 126 in good yields and diastereoselectivities. This methodology was successfully applied to the total synthesis of catharanthine 128 from the pre-functionalised indole lactam 127. Importantly, this approach features high stereocontrol and proceeds with rather low catalyst loading, likely a consequence of the more facile reduction of lactams versus acyclic amides.
When N-(trimethylsilyl)methyl amides 129 are employed, unstable azomethine ylides 133 are generated in situ via desilylation of 132 (Scheme 21). [44] 133 can be further trapped with dipolarophiles 130 via (3+2)-cycloaddition to afford highly functionalised pyrrolidines and pyrrolizidines 131. The reaction proceeds under mild conditions, enabling moderate to high diastereoselectivity and generally good compatibility with a variety of electron-deficient olefins.
As shown above, the reduction of amides 115 using Ir Icatalysed hydrosilylation usually affords the electrophilic iminium ion 120 as a key intermediate. By employing different trapping nucleophiles, Huang, Wang et al. were able to capture the iminium ion with different nucleophiles in various asymmetric catalytic systems (Scheme 22A). [45] Enantioselective reductive cyanation and phosphonylation reactions of secondary amides 134 were achieved using trimethylsilyl nitrile (TMSCN) or phosphites as the nucleophiles, in combination with chiral thiourea catalysts. A wide array of enantioenriched chiral α-aminonitriles 135 and αaminophosphonates 136 were prepared using this protocol.
The same groups later reported an asymmetric reductive alkynylation of amides using an elegant Ir/Cu relay catalysis manifold (Scheme 22B). [46] A wide scope of chiral propargylamines 139 were delivered in high yields and ee values. Nevertheless, the substrates are limited to the tertiary arylamides.

Nickel-Catalysed Amide Activation
While, as shown above, iridium can be broadly used to selectively reduce amides to give iminium ions, nickel(0) affords entirely different types of intermediates. The oxidative addition of electron-rich transition-metal complexes to destabilised amide CÀ N bonds leads to metallated intermediates that can be engaged in typical cross-coupling reactions. [8,47] The process of oxidative addition of Ni 0 to a CÀ N bond is also involved in a decarbonylation of Nacylated N-heteroarenes, [48] as well as a cyclisation reaction between aromatic amides and bicyclic alkenes, as recently described by the Chatani group. [49] In 2021, Garg et al. developed the first catalytic method for the direct intermolecular addition of two distinct nucleophiles to the carbonyl group of twisted amides 140 (Scheme 23). [50,51] Therein, a CÀ C bond and a CÀ H bond were formed sequentially, via Suzuki-Miyaura cross coupling followed by transfer hydrogenation, furnishing the secondary alcohols 141 in very good yields.
Although a variety of transformations, such as esterification, transamidation and Suzuki-Miyaura cross coupling, was achieved using similar strategies, prior to 2020, no conversion of twisted amides to the corresponding carboxylic acids had been reported. [8,47] To remedy this situation, Garg et al. developed an operationally simple procedure, once again employing Ni(cod) 2 as a pre-catalyst (Scheme 24). [52] A nickel-catalysed esterification of benzamides 142 with 2-(trimethylsilyl)ethanol 143 was first conducted, followed by fluoride-mediated deprotection in the same pot. Although this method offers a stepwise strategy to convert the tertiary benzamides 142 to the corresponding carboxylic acids 144, a straightforward transformation of more general amides is still highly required.

Amide Activation Catalysed by Lewis Acids
In a logic similar to that of electrophilic activation, transition-metal-based Lewis acids have also been employed to increase the electrophilicity of amides and have allowed subsequent nucleophilic attack. Based on prior work on transesterification, [53] Ballet and Maes et al. achieved a zinccatalysed chemoselective transamidation with a tert-butyl nicotinate (tBu-nic) 145 as a directing group (Scheme 25). [54] Inspired by metallo-exopeptidases in nature, the authors proposed that the designed directing group (tBu-nic) might allow bidentate chelation with a transition metal (146) and thus assists cleavage of a secondary amide under neutral and mild conditions. Notably, the tBu-nic-protected amide 145 is inert under typical peptide coupling/deprotection conditions, which enables its use as a potential building block in peptide synthesis. Furthermore, the authors applied this protocol to a macrocyclisation of a heptapeptide 148.
Ma and co-workers developed a tungsten(VI)-catalysed transamidation of tertiary alkyl amides 149 to secondary amides 151, using 1,10-phenanthroline as ligand with TMSCl as an additive (Scheme 26). [55] In this transformation, the tungsten catalyst activates the amide bond of tertiary alkyl amide 149 to form a cationic O-bound W-iminium species 152. Subsequent nucleophilic attack from amine 150 affords the tetrahedral intermediate 153. Intermediate 154, which is particularly favourable when a more protic aromatic amine or primary aromatic or alkylamine underwent transamidation, is given via proton transfer. The elimination of more basic dialkyl amine gives 155, which can further be transformed to the corresponding transamidated product 151. The authors also showed several limited examples on transamidation of tertiary alkyl amides with secondary amines.

Amide Functionalisations Initiated by Nucleophilic Addition
In spite of their poorly electrophilic character, amides can still be attacked by strong nucleophiles such as metal hydrides and alkyllithium reagents. The generated tetrahedral intermediate (see 164, Scheme 28) can be further reduced or functionalised. [9] Chiba et al. developed a strategy for the controlled reduction of carboxamides 157 to alcohols 158 or amines 159 employing zinc hydride, generated in situ by combining sodium hydride (NaH) and zinc halides (ZnX 2 ) (Scheme 27). [56] The nature of the halide on ZnX 2 was shown to afford different zinc hydride species, dictating the selectivity of the reduction. In the NaHÀ ZnI 2 system, polymeric zinc hydride (ZnH 2 ) is generated, deliver-ing alcohols. On the other hand, the NaHÀ ZnCl 2 system forms dimeric zinc chloride hydride (HÀ ZnÀ Cl) 2 and produces amines.
Later, Dixon, Chiba et al. described a reductive functionalisation of carboxamides 160 for the synthesis of αbranched amines 161 or 162 (Scheme 28). [57] Therein, a stable anionic hemiaminal intermediate 163 is formed through single hydride transfer from the sodium hydride/ sodium iodide composite. This species is then captured by TMSCl and the resulting activated hemiaminal 164. Elimination of trimethylsiloxide generates iminium ion 165, which can be attacked by other nucleophiles, such as Grignard reagents or cyanide, resulting in deoxygenative installation of a carbon substituent to afford α-branched amines 161 or 162. Although a valuable method due to the versatility of the amines that can be synthesised, this transformation is not chemoselective in presence of other carbonyl groups.
Using N-alkoxylactam derivatives 166 as substrates, Sato and Chida et al. developed a useful approach to access highly substituted cyclic nitrones 167 (Scheme 29). [58] This process was initiated by the nucleophilic attack of organolithium reagents to 166, with subsequent removal of the 2-(trimethylsilyl)ethoxymethyl (SEM) group under acidic conditions, furnishing the desired products 167. This approach was successfully applied to the total synthesis of cylindricine C 168. The key chiral nitrone intermediate 169 was afforded with the established method using hexenyl lithium. This intermediate 164 is able to undergo an intramolecular (3+2)-cycloaddition, giving desired tricyclic product 171 in 39 % yield. The regioselectivity of the cycloaddition step is poor and the major by-product is the undesired isomer 170.
Recently, Chiba and co-workers reported a protocol for the synthesis of α-tertiary amines 174 by iterative additions of carbon nucleophiles to amides (Scheme 30). [59] The proposed mechanism suggested that organolithium addition to the amide carbonyl 173 formed the anionic hemiaminal intermediate 175, which was detected by NMR analysis. Subsequent in situ O-silylation gave intermediate 176.
Eventually, the addition of Grignard reagent to the thus formed iminium ion 177 afforded the desired product.
A chemo-divergent transformation of primary, secondary and tertiary amides, as well as lactams 179, using 1,1diborylalkanes 180 as pro-nucleophiles was reported by the Liu group in 2020 (Scheme 31). [60] When primary and secondary amides or tertiary lactams are used as the starting Scheme 28. NaH/NaI-triggered reductive functionalisation of tertiary amides into α-branched amines 161 and 162.

Scheme 29.
Nucleophilic approach to access highly substituted cyclic nitrones 167 from N-alkoxylactams 166 and its application in the total synthesis of cylindricine C. Ketones 184 are afforded via in situ hydrolysis of these intermediates. Trapped by trifluoroacetic anhydride, the enamine intermediates 185 allow the synthesis of enamides 186 from primary amides. This method provides different possibilities of functionalisations of amides. However, the need for an organolithium to activate the 1,1-diborylalkane pronucleophile might restrict chemoselectivity.

Amide Activation and Functionalisation with SmI 2 /Sm
Electron transfer to carboxylic acid derivatives mediated by Sm II is a well-established and powerful strategy to invert the polarity of the carbonyl group, resulting in the formation of a carbon-centred radical and/or a dianion (Schemes 32 and 33). Wang et al. showed that SmI 2 /Sm-mediated umpolung of the carbonyl carbon of amide 187 generated an intermediate (191) capable of reacting with aryl pinacolboronate ester 188 (Scheme 32). [61] Subsequent boron 1,2-metalate rearrangement and protodeboronation provided the corresponding arylmethylamines 189 as the products of deoxygenative CÀ C bond coupling. The authors also showed that the use of catalytic amounts of Pd(PPh 3 ) 4 dramatically increases the yield of the reaction.
A deoxygenative cross-coupling reaction of amides 193 with polyfluoroarenes 194, promoted by SmI 2 /Sm, was reported by the same group (Scheme 33). [62] This transformation affords the α-polyfluoroaryl amines 195 in moderate to good yields through what amounts to a direct CÀ H functionalisation of polyfluoroarenes 194. The authors proposed carbon-centred radical low-valence Sm II species 198 to be one of the key intermediates of this process.

Conclusion and Outlook
By exploiting the intrinsic electronic and geometric properties of amides, selective amide activation protocols have delivered highly versatile tools to functionalise amides or to convert them into entirely different functional groups. Given the amount of new highly visible publications within the relatively short timeframe covered by this Minireview, it is apparent that amide activation enjoys high interest within the synthetic community. Recent breakthroughs tackled some of the most challenging limitations, such as functionalisation at the "nitrogen part" of amides or the establishment of organocatalytic approaches. Furthermore, new endeavours have been made towards remote functionalisation, stereoselective transformations and overall amide functionalisation strategies. Although important progress has been made, considerable limitations and challenges still exist. First and foremost, there is a clear need to develop even more general approaches. For some of the methods, the reaction scope is limited to specific amides such as tertiary benzamide derivatives. Additionally, while many methods for amide activation are already highly chemoselective, certain transformations still suffer from competition by other carbonyl derivatives or nucleophilic functionality. Notably, the implementation of enantioselective variants remains a highly challenging goal. Considering the recent breakthroughs and the current limitations, amide activation offers a vast field for additional explorations further challenging the conventional, by now perhaps outdated, view of this functional group.